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1-[4-(hydroxymethyl)-1H-1,2,3-triazol-1-yl]-3-phenoxypropan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1452855-83-2

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1452855-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1452855-83-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,2,8,5 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1452855-83:
(9*1)+(8*4)+(7*5)+(6*2)+(5*8)+(4*5)+(3*5)+(2*8)+(1*3)=182
182 % 10 = 2
So 1452855-83-2 is a valid CAS Registry Number.

1452855-83-2Downstream Products

1452855-83-2Relevant academic research and scientific papers

Doped Nano-Sized Copper(I) Oxide (Cu2O) on melamine-formaldehyde resin: A highly efficient heterogeneous nano catalyst for 'Click' synthesis of some novel 1h-1,2,3-triazole derivatives having antibacterial activity

Rad, Mohammad Navid Soltani,Behrouz, Somayeh,Movahedian, Abdollah,Doroodmand, Mohammad Mahdi,Ghasemi, Younes,Rasoul-Amini, Sara,Gandomani, Abdol-Rasoul Ahmadi,Rezaie, Ramin

, p. 688 - 701 (2013/05/22)

A facile and simple protocol for the 1,3-dipolar cycloaddition of organic azides with terminal alkynes catalyzed by doped nano-sized Cu2O on melamine-formaldehyde resin (nano-Cu2O-MFR) as a new and convenient heterogeneous catalyst is described. In this method, 'click' cycloaddition of various structurally diverse β-azido alcohols and alkynes in the presence of nano-Cu2O-MFR in H2O/THF 1: 2 furnished the corresponding 1,4-disubstituted 1H-1,2,3-triazole adducts 1a-1o in good to excellent yields at room temperature (Scheme and Table 3). The nano-Cu 2O-MFR was characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), inductively coupled plasma (ICP) analysis, and FT-IR. The nano-Cu2O-MFR could be easily recovered and recycled from the reaction mixture and reused for many consecutive trials without significant decrease in activity (Table 4). The in vitro antibacterial activities of all synthesized compounds were tested on several Gram-positive and/or Gram-negative bacteria (Table 5). The results demonstrate the promising antibacterial activity for some of the synthesized compounds. Copyright

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